Design an AI-enabled software as a medical device that offers cutting-edge capabilities and earns the trust of healthcare professionals, ultimately improving patient care.
5 tips for designing AI-enabled SaMD that HCPs trust
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Yvette Granger
Managing Partner
Yvette’s background is in human factors engineering and human-system integration (HSI) research. She has designed methodologies, defined project scope, planned research activities, and supervised programs of research as well as individual research projects involving medical devices, touch screen interfaces, websites, and enterprise applications. In her most recent role, Yvette managed the Human Factors research programs for multi-million-dollar client accounts within the healthcare sector. She is a member of HFES, AAMI, and the Epsilon Mu Eta honor society. Yvette has an MS in Engineering Management with a certificate in HSI from the University of Missouri.
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Yvette
Something unique about you summed up in one sentence
I enjoy the musical stylings of Dethklok and Ed Sheeran equally
Your favorite part of working at Bold Insight
The people (this team is incredible) and the work (we make a difference every single day)!
In your spare time (or if you had spare time), you would absolutely do this:
Flip houses à la Chip and Joanna Gaines
How long have you been in the UX field?
10+ years
You cannot start the day without doing this...
Checking the weather. Living in the Chicago area has made me this way!
Your favorite city in the world is...and why?
Sydney in the Summer – the sights, the food, the ocean, and the energy!
Your ultimate celebrity dinner party guest list would include:
Barack Obama, Ozzy Osbourne, Neil Gaiman, and Terry Pratchett
Long-term personal or professional goal?
To achieve the perfect work-life balance
Read Yvette's bold insights
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This year marks the 20th anniversary of the UXalliance. To celebrate this milestone, we sat down with Gavin, one of the five founding members, to discuss the organization’s history, guiding principles, and the benefits it brings to clients.
Human factors testing for OTC drugs and non-prescription medical devices
As the field of human factors continues to evolve, so must our approaches to testing and study design. While the FDA’s 2013 guidance laid the groundwork for study design and methodology, recent discussions and conference presentations have prompted a shift in how we approach OTC HF testing, leading to more comprehensive and realistic assessments of these products.